JP2015517484A5 - - Google Patents

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Publication number
JP2015517484A5
JP2015517484A5 JP2015510875A JP2015510875A JP2015517484A5 JP 2015517484 A5 JP2015517484 A5 JP 2015517484A5 JP 2015510875 A JP2015510875 A JP 2015510875A JP 2015510875 A JP2015510875 A JP 2015510875A JP 2015517484 A5 JP2015517484 A5 JP 2015517484A5
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JP
Japan
Prior art keywords
seq
pharmaceutical composition
sequence
peptide
pharmaceutically acceptable
Prior art date
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JP2015510875A
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Japanese (ja)
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JP2015517484A (en
JP5982562B2 (en
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Publication date
Priority claimed from GB201208293A external-priority patent/GB201208293D0/en
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Publication of JP2015517484A publication Critical patent/JP2015517484A/en
Publication of JP2015517484A5 publication Critical patent/JP2015517484A5/ja
Application granted granted Critical
Publication of JP5982562B2 publication Critical patent/JP5982562B2/en
Expired - Fee Related legal-status Critical Current
Anticipated expiration legal-status Critical

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Claims (13)

CPAVKRDVDLFLT (SEQ ID NO: 1)の配列から成るペプチドの塩酸塩。   Peptide hydrochloride consisting of the sequence CPAVKRDVDLFLT (SEQ ID NO: 1). 5質量%未満の(a)SEQ ID NO: 1の配列から成るペプチドからの末端システイン-プロリン残基の開裂により生じる不純物を含む請求項1記載の塩。 The salt according to claim 1 , comprising less than 5% by weight of (a) an impurity resulting from cleavage of a terminal cysteine-proline residue from a peptide consisting of the sequence of SEQ ID NO: 1. 5質量%未満の(b)SEQ ID NO: 1の配列から成るペプチドのシステインスルフィン酸形態及び/又は(c)SEQ ID NO: 1の配列から成るペプチドのダイマーを含む請求項1又は2記載の塩。 5 wt% less than (b) SEQ ID NO: of the peptide consisting of 1 of SEQ cysteine sulfinic acid form and / or (c) SEQ ID NO: according to claim 1 or 2, wherein comprising the dimer of a peptide consisting of one of the sequences salt. 請求項1から3のいずれか1項に記載の塩酸塩及び医薬的に許容可能な担体又は希釈剤を含有する医薬組成物。   A pharmaceutical composition comprising the hydrochloride according to any one of claims 1 to 3 and a pharmaceutically acceptable carrier or diluent. 更に追加のペプチド1種以上又はそれらの医薬的に許容可能な塩を含有する請求項4記載の医薬組成物。   The pharmaceutical composition according to claim 4, further comprising one or more additional peptides or a pharmaceutically acceptable salt thereof. 該追加のペプチド1種以上又はそれらの医薬的に許容可能な塩が、SEQ ID NO: 2から7の配列から成るペプチド又はそれらの医薬的に許容可能な塩から選択される請求項5記載の医薬組成物。   6. The one or more additional peptides or pharmaceutically acceptable salts thereof are selected from peptides consisting of the sequence of SEQ ID NO: 2 to 7 or pharmaceutically acceptable salts thereof. Pharmaceutical composition. 該追加のペプチド1種以上又はそれらの医薬的に許容可能な塩が、SEQ ID NO: 2から7の配列から成る6種のペプチド又はそれらの医薬的に許容可能な塩である請求項6記載の医薬組成物。   7. The one or more additional peptides or pharmaceutically acceptable salts thereof are six peptides consisting of the sequence of SEQ ID NO: 2 to 7, or pharmaceutically acceptable salts thereof. Pharmaceutical composition. ・チオグリセロール、チオアニソール又はメチオニンの少なくとも1種;及び/又は
・トレハロース又はショ糖の少なくとも1種
を更に含む請求項7記載の医薬組成物。
The pharmaceutical composition according to claim 7, further comprising at least one of thioglycerol, thioanisole or methionine; and / or at least one of trehalose or sucrose.
・SEQ ID NO: 1の配列から成るペプチドの塩酸塩;
・SEQ ID NO: 2から7の配列から成る6種のペプチドの酢酸塩;
・トレハロース;
・チオグリセロール;
・メチオニン及び任意成分として、
・リン酸
を含む請求項7又は8記載の医薬組成物。
The hydrochloride salt of the peptide consisting of the sequence SEQ ID NO: 1;
SEQ ID NO: 6 peptide acetates consisting of sequences 2 to 7;
・ Trehalose;
Thioglycerol;
・ As methionine and optional ingredients
-Pharmaceutical composition of Claim 7 or 8 containing phosphoric acid.
5質量%未満の(a)SEQ ID NO: 1の配列から成るペプチドからの末端システイン-プロリン残基の開裂により生じる不純物を含む請求項4から9のいずれか1項に記載の医薬組成物。 10. A pharmaceutical composition according to any one of claims 4 to 9, comprising less than 5% by weight of (a) an impurity resulting from cleavage of a terminal cysteine-proline residue from a peptide consisting of the sequence of SEQ ID NO: 1. 5質量%未満の(b)SEQ ID NO: 1の配列から成るペプチドのシステインスルフィン酸形態及び/又は(c)SEQ ID NO: 1の配列から成るペプチドのダイマーを含む請求項4から10のいずれか1項に記載の医薬組成物。 11. A composition according to any of claims 4 to 10, comprising less than 5% by weight of (b) a cysteine sulfinic acid form of a peptide consisting of the sequence of SEQ ID NO: 1 and / or (c) a peptide dimer consisting of the sequence of SEQ ID NO: 1. 2. A pharmaceutical composition according to claim 1. 求項1から3のいずれか1項に記載の塩酸塩を活性成分として含む、ネコに対するアレルギーの予防又は治療剤From Motomeko 1 comprising as active ingredient the hydrochloride salt according to any one of 3, prophylactic or therapeutic agent for allergy to cats. 求項4から11のいずれか1項に記載の医薬組成物を活性成分として含む、ネコに対するアレルギーの予防又は治療剤 Motomeko including 4 from the pharmaceutical composition according to any one of 11 as an active ingredient, a preventive or therapeutic agent for allergy to cats.
JP2015510875A 2012-05-11 2013-05-09 Peptide hydrochloride and its immunotherapy use in combination with other peptides Expired - Fee Related JP5982562B2 (en)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
GB201208293A GB201208293D0 (en) 2012-05-11 2012-05-11 Hydrochlorice salt of peptide
GB1208293.9 2012-05-11
PCT/GB2013/051201 WO2013167897A1 (en) 2012-05-11 2013-05-09 Hydrochloride salt of peptide and its use in combination with other peptides for immunotherapy

Publications (3)

Publication Number Publication Date
JP2015517484A JP2015517484A (en) 2015-06-22
JP2015517484A5 true JP2015517484A5 (en) 2016-06-30
JP5982562B2 JP5982562B2 (en) 2016-08-31

Family

ID=46396890

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2015510875A Expired - Fee Related JP5982562B2 (en) 2012-05-11 2013-05-09 Peptide hydrochloride and its immunotherapy use in combination with other peptides

Country Status (17)

Country Link
US (1) US9657061B2 (en)
EP (1) EP2847209B8 (en)
JP (1) JP5982562B2 (en)
KR (1) KR20150014955A (en)
CN (1) CN104428311B (en)
AU (1) AU2013257784A1 (en)
BR (1) BR112014028130A2 (en)
CA (1) CA2873120A1 (en)
EA (1) EA201492068A1 (en)
GB (2) GB201208293D0 (en)
HK (1) HK1201850A1 (en)
IL (1) IL235388A (en)
IN (1) IN2014DN09367A (en)
MX (1) MX2014013394A (en)
SG (1) SG11201407446TA (en)
WO (1) WO2013167897A1 (en)
ZA (1) ZA201408290B (en)

Families Citing this family (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB201406569D0 (en) 2014-04-11 2014-05-28 Stabilitech Ltd Vaccine compositions
GB201501017D0 (en) * 2014-12-23 2015-03-04 Immatics Biotechnologies Gmbh Novel peptides and combination of peptides for use in immunotherapy against hepatocellular carcinoma (HCC) and other cancers
DK3236985T4 (en) 2014-12-23 2022-11-28 Immatics Biotechnologies Gmbh PREVIOUSLY UNKNOWN PEPTIDES AND COMBINATION OF PEPTIDES FOR USE IN IMMUNOTHERAPY AGAINST HEPATOCELLULAR CARCINOMA (HCC) AND OTHER CANCER
GB201505305D0 (en) 2015-03-27 2015-05-13 Immatics Biotechnologies Gmbh Novel Peptides and combination of peptides for use in immunotherapy against various tumors
GB2562241B (en) 2017-05-08 2022-04-06 Stabilitech Biopharma Ltd Vaccine compositions
TWI792442B (en) * 2021-07-23 2023-02-11 建誼生技股份有限公司 Method for preparing etelcalcetide hydrochloride

Family Cites Families (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
ATE414534T1 (en) * 2001-12-05 2008-12-15 Circassia Ltd IMMUNOTHERAPEUTIC METHODS AND SYSTEMS
KR101728868B1 (en) * 2006-01-18 2017-05-02 포시 파마슈티컬스 컴퍼니 리미티드 Pharmaceutical compositions with enhanced stability
GB0710529D0 (en) 2007-06-01 2007-07-11 Circassia Ltd Vaccine
PT2083856E (en) * 2007-08-15 2010-12-23 Circassia Ltd Peptides for desensibilization against allergens
GB2455108A (en) * 2007-11-28 2009-06-03 Circassia Ltd T-Cell dependent method for detecting non-allergic or intrinsic disorders
GB0821806D0 (en) * 2008-11-28 2009-01-07 Circassia Ltd Compositions with reduced dimer formation
HUE033656T2 (en) * 2010-03-31 2017-12-28 Stabilitech Ltd Excipients for stabilising viral particles

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